ReviewNaunyn-Schmiedeberg's archives of pharmacology2026
Datopotamab deruxtecan for endocrine-resistant HR-positive/HER2-negative breast cancer: biological rationale and clinical evidence.
Review in Naunyn-Schmiedeberg's archives of pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
2 authors.
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Abstract
Hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR-positive/HER2-negative) breast cancer is primarily managed with endocrine-based therapies; however, resistance to endocrine therapy and CDK4/6 inhibitors commonly develops in advanced disease. Following treatment failure, therapeutic options are largely limited to sequential chemotherapy, which provides modest clinical benefit and is associated with cumulative toxicity. Antibody-drug conjugates (ADCs) targeting trophoblast cell surface antigen 2 (TROP-2) have emerged as a promising strategy for delivering cytotoxic agents selectively to tumor cells in endocrine-refractory disease. This narrative review summarizes current evidence on the biological rationale, pharmacologic characteristics, and clinical development of datopotamab deruxtecan (Dato-DXd), with emphasis on findings from the phase III TROPION-Breast01 trial and relevant translational studies. Datopotamab deruxtecan is a TROP-2-directed ADC that enables targeted delivery of a potent topoisomerase I inhibitor payload to tumor cells. In the TROPION-Breast01 trial, Dato-DXd demonstrated a statistically significant improvement in progression-free survival compared with investigator's choice chemotherapy in patients with endocrine-refractory HR-positive/HER2-negative metastatic breast cancer. Clinical activity was observed across heterogeneous TROP-2 expression, including in heavily pretreated patients and those with visceral disease. Hematologic toxicity was relatively limited, although interstitial lung disease remains an important safety consideration requiring proactive monitoring. Datopotamab deruxtecan represents a clinically meaningful therapeutic option based on the targeted delivery of cytotoxic chemotherapy for patients with endocrine-resistant HR-positive/HER2-negative breast cancer. Ongoing studies are required to define optimal treatment sequencing, combination strategies, and long-term safety outcomes.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.